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Published Apr 24, 23
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Publisher Copyright: extcopyright 2021, The Author(s), under exclusive licence to Springer Nature Switzerland AG. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.", year = "2021", month = oct, doi = "10. 1007/s40266-021-00882-2", language = "English", volume = "38", pages = "887--910", journal = "Drugs and Aging", issn = "1170-229X", publisher = "Adis International Ltd", number = "10",TY - JOURT1 - Safety and Tolerability of Natural and Synthetic Cannabinoids in Older Adults, T2 - A Systematic Review and Meta-Analysis of Open-Label Trials and Observational Studies, AU - Pisani, Sara, AU - Mc, Goohan, Katie, AU - Velayudhan, Latha, AU - Bhattacharyya, Sagnik, N1 - Funding Information: SB and LV received funding from Parkinson’s UK (grant number G-1901).

16/126/53]. The authors acknowledge support from the National Institute for Health Research Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King’s College London. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. No other disclosures were reported.

Copyright: Copyright 2021 Elsevier B.V., All rights reserved. PY - 2021/10Y1 - 2021/10N2 - BACKGROUND AND OBJECTIVE: Although cannabinoid-based medications are increasingly used by older adults, their safety and tolerability in this age group remain unclear. The purpose of this systematic review was to examine the safety and tolerability of cannabinoid-based medications by conducting a meta-analysis of open-label observational studies of cannabinoid-based medications for all indications in individuals with a mean age of ≥50 years.

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CBD for Parkinson's Disease Symptoms   APDAThe endocannabinoid system – current implications for drug development - Fowler - 2021 - Journal of Internal Medicine - Wiley Online Library

Study quality was assessed using an adapted version of the Grading of Recommendations Assessment, Development and Evaluation criteria and Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines were followed. We included studies that (a) were published from 1990 onwards; (b) included older adults (mean age ≥50 years); and (c) provided data on the safety and tolerability of medical cannabinoids.

Risk of adverse events, serious adverse events and withdrawals was computed as the incidence rate (IR). Separate analyses were conducted by the cannabinoid-based medication used, for delta-9-tetrahydrocannabinol (THC), cannabidiol (CBD) and a combination of THC and CBD (THC:CBD). RESULTS: Thirty-eight studies were identified (THC = 23; CBD = 6; THC:CBD = 9; N = 2341, mean age: 63.

Frontiers   Translational Investigation of the Therapeutic Potential of  Cannabidiol (CBD): Toward a New AgeCannabidiol use and effectiveness: real-world evidence from a Canadian medical cannabis clinic Journal of Cannabis Research Full Text

08 years, men: 53. 86%). THC had a very low incidence of all-cause and treatment-related adverse events (IR: 122. 18, 95% confidence interval [CI] 38. 23-253. 56; IR: 84. 76, 95% CI 0. 13-326. 01, respectively) and negligible serious adverse events (IR = 0). Similar IRs for CBD (all cause, IR: 111.

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Higher Risk, Higher Reward? Self‐Reported Effects of Real‐World Cannabis  Use in Parkinson's Disease - Holden - 2022 - Movement Disorders Clinical  Practice - Wiley Online LibraryCBD oil and Parkinson's disease

24-495. 93; treatment related, IR: 1. 76, 95% CI 4. 63-23. 05) and no serious adverse events (IR = 0). CBD was not associated with a risk of treatment-related withdrawals. THC had a low risk of all-cause and treatment-related withdrawals (IR: 25. 18, 95% CI 12. 35-42. 52; IR: 7.

PDF) Cannabinoids in the Treatment of Parkinson's DiseaseHigher Risk, Higher Reward? Self‐Reported Effects of Real‐World Cannabis Use in Parkinson's Disease - Holden - 2022 - Movement Disorders Clinical Practice - Wiley Online Library

26-14. 38, respectively). The THC:CBD treatment had a low risk of all-cause and treatment-related adverse events (IR: 100. 72, 95% CI 0. 25-383. 00; IR: 55. 38, 95% CI 8. 61-142. 80, respectively), but reported a risk of all-cause and treatment-related serious adverse events (IR: 21. 32, 95% CI 0.

26; IR: 3. 71, 95% CI 0. 21-11. 56, respectively), and all-cause and treatment-related withdrawals (IR: 78. 63, 95% CI 17. 43-183. 90; IR: 34. 31, 95% CI 6. 09-85. 52, respectively). Significant heterogeneity (I2 >55%) was present in most analyses. CONCLUSIONS: Although cannabinoid-based medications were generally safe and acceptable to adults aged over 50 years, these estimates are limited by the lack of a control condition and considerable heterogeneity.

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AB - BACKGROUND AND OBJECTIVE: Although cannabinoid-based medications are increasingly used by older adults, their safety and tolerability in this age group remain unclear. The purpose of this systematic review was to examine the safety and tolerability of cannabinoid-based medications by conducting a meta-analysis of open-label observational studies of cannabinoid-based medications for all indications in individuals with a mean age of ≥50 years.



Study quality was assessed using an adapted version of the Grading of Recommendations Assessment, Development and Evaluation criteria and Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines were followed. We included studies that (a) were published from 1990 onwards; (b) included older adults (mean age ≥50 years); and (c) provided data on the safety and tolerability of medical cannabinoids.

Risk of adverse events, serious adverse events and withdrawals was computed as the incidence rate (IR). Separate analyses were conducted by the cannabinoid-based medication used, for delta-9-tetrahydrocannabinol (THC), cannabidiol (CBD) and a combination of THC and CBD (THC:CBD). RESULTS: Thirty-eight studies were identified (THC = 23; CBD = 6; THC:CBD = 9; N = 2341, mean age: 63.

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